Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA.
Impairment of the ability to coordinate the movements required for normal ambulation (WALKING) which may result from impairments of motor function or sensory feedback. This condition may be associated with BRAIN DISEASES (including CEREBELLAR DISEASES and BASAL GANGLIA DISEASES); SPINAL CORD DISEASES; or PERIPHERAL NERVOUS SYSTEM DISEASES.
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
The coordination of a sensory or ideational (cognitive) process and a motor activity.

Non-motor associative learning in patients with isolated degenerative cerebellar disease. (1/486)

In recent decades it has become clear that the cerebellum is involved in associative motor learning, but its exact role in motor learning as such is still controversial. Recently, a contribution of the cerebellum to different cognitive abilities has also been considered, but it remains unclear whether the cerebellum contributes to cognitive associative learning. We compared nine patients with an isolated cerebellar degenerative disease in a cognitive associative learning task with 10 controls. Patients and controls were matched for age, sex, handedness, level of education, intelligence and capabilities of visual memory. The subjects were asked to learn the association between six pairs of colours and numerals by trial and error. Additionally, a simple reaction time and a visual scanning test were conducted in order to control for the influence of motor performance deficits in cerebellar patients. In comparison with the controls, it took the patients significantly longer to learn the correct associations between colours and numerals, and they were impaired in recognizing them later on. Two patients showed no associative learning effect at all. Neither the simple reaction time nor the visual scanning time correlated substantially with the results of associative learning. Therefore, motor-associated disabilities are unlikely to be the reason for the learning deficit in cerebellar patients. Our results suggest that the cerebellum might contribute to motor-independent processes that are generally involved in associative learning.  (+info)

Contralateral deafness following unilateral suboccipital brain tumor surgery in a patient with large vestibular aqueduct--case report. (2/486)

A 68-year-old female developed contralateral deafness following extirpation of a left cerebellopontine angle epidermoid cyst. Computed tomography showed that large vestibular aqueduct was present. This unusual complication may have been caused by an abrupt pressure change after cerebrospinal fluid release, which was transmitted through the large vestibular aqueduct and resulted in cochlear damage.  (+info)

Anticonvulsant-induced dyskinesias: a comparison with dyskinesias induced by neuroleptics. (3/486)

Anticonvulsants cause dyskinesias more commonly than has been appreciated. Diphenylhydantoin (DPH), carbamazepine, primidone, and phenobarbitone may cause asterixis. DPH, but not other anticonvulsants, may cause orofacial dyskinesias, limb chorea, and dystonia in intoxicated patients. These dyskinesias are similar to those caused by neuroleptic drugs and may be related to dopamine antagonistic properties possessed by DPH.  (+info)

Intrameatal aneurysm successfully treated by meatal loop trapping--case report. (4/486)

A 77-year-old female presented with a rare intrameatal aneurysm manifesting as sudden onset of headache, hearing loss, tinnitus, and vertigo associated with subarachnoid hemorrhage. Meatal loop trapping was performed. After surgery, the patient's functions recovered almost completely, probably because of the preservation of the 7th and 8th cranial nerves and the presence of effective collaterals in the area supplied by the anterior inferior cerebellar artery.  (+info)

Remote regional cerebral blood flow consequences of focused infarcts of the medulla, pons and cerebellum. (5/486)

The aim of this study was to evaluate regional and remote diaschisis of inferior brain stem or cerebellar infarcts in 25 patients presenting with relatively limited lesions. Patients presented with medullary, pontine or cerebellar infarction. METHODS: Lesions were evaluated on MRI (0.5 T). Regional cerebral blood flow (rCBF) was assessed by means of SPECT, after injection of 9rmTc-hexamethyl propyleneamine oxime (HMPAO) and, when possible, inhalation of 133Xe in the same session. For each method, asymmetry indices (Als), comparing contralateral to ipsilateral rCBF values, were calculated in four areas of each cerebral hemisphere and in the cerebellum and later compared with values obtained in healthy subjects (P = 0.05). RESULTS: Higher rCBF values were observed in the contralateral cerebellum in 2 of 7 patients with selective lateral medullary lesions, and cerebellar Als were significantly increased. When a cerebellar infarct was associated with a lateral medullary lesion, the cerebellar and contralateral hemispheric asymmetries were more severe. Unilateral paramedian pontine infarcts had more frequent consequences on the cerebellum (2 of 3 cases), with rCBF or tracer uptake being reduced in the ipsilateral or the contralateral lobe. Inverse cerebral hemispheric asymmetry could then be observed. Bilateral pontine lesions were difficult to evaluate. Using 99mTc-HMPAO, discrete cerebellar asymmetry was observed in 3 of 6 cases. Pure cerebellar infarcts in the posterior inferior cerebellar artery territory were always associated with a severe ipsilateral flow drop in the cerebellum, and contralateral hemispheric diaschisis was frequent (3 of 4 patients), predominating in the frontotemporal cortex and subcortical structures. This was also more obvious using 99mTC-HMPAO than 133Xe. Variance analysis showed that hemispheric diaschisis was more severe in mixed brain stem and cerebellar infarcts than in pure cerebellar or brain stem lesions. Furthermore, cerebellar and hemispheric AI values were not correlated with measurements of clinical deficits, disability or handicap. CONCLUSION: Unilateral and limited inferior brain stem lesions can have ipsi- or contralateral consequences on the cerebellum and cerebral hemispheres rCBF. These remote effects are related to lesions of the main pathways joining these structures, resulting in deactivation and, in some cases, overactivation. Contrary to what has been suggested, consequences on cerebral hemispheres are more severe in mixed cerebellar and brain stem infarcts than in pure cerebellar lesions.  (+info)

Multiple large and small cerebellar infarcts. (6/486)

To assess the clinical, topographical, and aetiological features of multiple cerebellar infarcts,18 patients (16.5% of patients with cerebellar infarction) were collected from a prospective acute stroke registry, using a standard investigation protocol including MRI and magnetic resonance angiography. Infarcts in the posterior inferior cerebellar artery (PICA)+superior cerebellar artery (SCA) territory were most common (9/18; 50%), followed by PICA+anterior inferior cerebellar artery (AICA)+SCA territory infarcts (6/18; 33%). One patient had bilateral AICA infarcts. No infarct involved the PICA+AICA combined territory. Other infarcts in the posterior circulation were present in half of the patients and the clinical presentation largely depended on them. Large artery disease was the main aetiology. Our findings emphasised the common occurrence of very small multiple cerebellar infarcts (<2 cm diameter). These very small multiple cerebellar infarcts may occur with (13 patients/18; 72%) or without (3/18; 22%) territorial cerebellar infarcts. Unlike previous series, they could not all be considered junctional infarcts (between two main cerebellar artery territories: 51/91), but also small territorial infarcts (40/91). It is suggested that these very small territorial infarcts may be endzone infarcts, due to the involvement of small distal arterial branches. It is possible that some very small territorial infarcts may be due to a microembolic process, but this hypothesis needs pathological confirmation.  (+info)

Failure of cerebellar patients to time finger opening precisely causes ball high-low inaccuracy in overarm throws. (7/486)

We investigated the idea that the cerebellum is required for precise timing of fast skilled arm movements by studying one situation where timing precision is required, namely finger opening in overarm throwing. Specifically, we tested the hypothesis that in overarm throws made by cerebellar patients, ball high-low inaccuracy is due to disordered timing of finger opening. Six cerebellar patients and six matched control subjects were instructed to throw tennis balls at three different speeds from a seated position while angular positions in three dimensions of five arm segments were recorded at 1,000 Hz with the search-coil technique. Cerebellar patients threw more slowly than controls, were markedly less accurate, had more variable hand trajectories, and showed increased variability in the timing, amplitude, and velocity of finger opening. Ball high-low inaccuracy was not related to variability in the height or direction of the hand trajectory or to variability in finger amplitude or velocity. Instead, the cause was variable timing of finger opening and thereby ball release occurring on a flattened arc hand trajectory. The ranges of finger opening times and ball release times (timing windows) for 95% of the throws were on average four to five times longer for cerebellar patients; e.g., across subjects mean ball release timing windows for throws made under the medium-speed instruction were 11 ms for controls and 55 ms for cerebellar patients. This increased timing variability could not be explained by disorder in control of force at the fingers. Because finger opening in throwing is likely controlled by a central command, the results implicate the cerebellum in timing the central command that initiates finger opening in this fast skilled multijoint arm movement.  (+info)

Preserved performance by cerebellar patients on tests of word generation, discrimination learning, and attention. (8/486)

Recent theories suggest that the human cerebellum may contribute to the performance of cognitive tasks. We tested a group of adult patients with cerebellar damage attributable to stroke, tumor, or atrophy on four experiments involving verbal learning or attention shifting. In experiment 1, a verb generation task, participants produced semantically related verbs when presented with a list of nouns. With successive blocks of practice responding to the same set of stimuli, both groups, including a subset of cerebellar patients with unilateral right hemisphere lesions, improved their response times. In experiment 2, a verbal discrimination task, participants learned by trial and error to pick the target words from a set of word pairs. When age was taken into account, there were no performance differences between cerebellar patients and control subjects. In experiment 3, measures of spatial attention shifting were obtained under both exogenous and endogenous cueing conditions. Cerebellar patients and control subjects showed similar costs and benefits in both cueing conditions and at all SOAs. In experiment 4, intra- and interdimensional shifts of nonspatial attention were elicited by presenting word cues before the appearance of a target. Performance was substantially similar for cerebellar patients and control subjects. These results are presented as a cautionary note. The experiments failed to provide support for current hypotheses regarding the role of the cerebellum in verbal learning or attention. Alternative interpretations of previous results are discussed.  (+info)

Cerebellar diseases refer to a group of medical conditions that affect the cerebellum, which is the part of the brain located at the back of the head, below the occipital lobe and above the brainstem. The cerebellum plays a crucial role in motor control, coordination, balance, and some cognitive functions.

Cerebellar diseases can be caused by various factors, including genetics, infections, tumors, stroke, trauma, or degenerative processes. These conditions can result in a wide range of symptoms, such as:

1. Ataxia: Loss of coordination and unsteady gait
2. Dysmetria: Inability to judge distance and force while performing movements
3. Intention tremors: Shaking or trembling that worsens during purposeful movements
4. Nystagmus: Rapid, involuntary eye movement
5. Dysarthria: Speech difficulty due to muscle weakness or incoordination
6. Hypotonia: Decreased muscle tone
7. Titubation: Rhythmic, involuntary oscillations of the head and neck
8. Cognitive impairment: Problems with memory, attention, and executive functions

Some examples of cerebellar diseases include:

1. Ataxia-telangiectasia
2. Friedrich's ataxia
3. Multiple system atrophy (MSA)
4. Spinocerebellar ataxias (SCAs)
5. Cerebellar tumors, such as medulloblastomas or astrocytomas
6. Infarctions or hemorrhages in the cerebellum due to stroke or trauma
7. Infections, such as viral encephalitis or bacterial meningitis
8. Autoimmune disorders, like multiple sclerosis (MS) or paraneoplastic syndromes
9. Metabolic disorders, such as Wilson's disease or phenylketonuria (PKU)
10. Chronic alcoholism and withdrawal

Treatment for cerebellar diseases depends on the underlying cause and may involve medications, physical therapy, surgery, or supportive care to manage symptoms and improve quality of life.

Gait ataxia is a type of ataxia, which refers to a lack of coordination or stability, specifically involving walking or gait. It is characterized by an unsteady, uncoordinated, and typically wide-based gait pattern. This occurs due to dysfunction in the cerebellum or its connecting pathways, responsible for maintaining balance and coordinating muscle movements.

In gait ataxia, individuals often have difficulty with controlling the rhythm and pace of their steps, tend to veer or stagger off course, and may display a reeling or stumbling motion while walking. They might also have trouble performing rapid alternating movements like quickly tapping their foot or heel. These symptoms are usually worse when the person is tired or attempting to walk in the dark.

Gait ataxia can be caused by various underlying conditions, including degenerative neurological disorders (e.g., cerebellar atrophy, multiple sclerosis), stroke, brain injury, infection (e.g., alcoholism, HIV), or exposure to certain toxins. Proper diagnosis and identification of the underlying cause are essential for effective treatment and management of gait ataxia.

Cerebellar ataxia is a type of ataxia, which refers to a group of disorders that cause difficulties with coordination and movement. Cerebellar ataxia specifically involves the cerebellum, which is the part of the brain responsible for maintaining balance, coordinating muscle movements, and regulating speech and eye movements.

The symptoms of cerebellar ataxia may include:

* Unsteady gait or difficulty walking
* Poor coordination of limb movements
* Tremors or shakiness, especially in the hands
* Slurred or irregular speech
* Abnormal eye movements, such as nystagmus (rapid, involuntary movement of the eyes)
* Difficulty with fine motor tasks, such as writing or buttoning a shirt

Cerebellar ataxia can be caused by a variety of underlying conditions, including:

* Genetic disorders, such as spinocerebellar ataxia or Friedreich's ataxia
* Brain injury or trauma
* Stroke or brain hemorrhage
* Infections, such as meningitis or encephalitis
* Exposure to toxins, such as alcohol or certain medications
* Tumors or other growths in the brain

Treatment for cerebellar ataxia depends on the underlying cause. In some cases, there may be no cure, and treatment is focused on managing symptoms and improving quality of life. Physical therapy, occupational therapy, and speech therapy can help improve coordination, balance, and communication skills. Medications may also be used to treat specific symptoms, such as tremors or muscle spasticity. In some cases, surgery may be recommended to remove tumors or repair damage to the brain.

Psychomotor performance refers to the integration and coordination of mental processes (cognitive functions) with physical movements. It involves the ability to perform complex tasks that require both cognitive skills, such as thinking, remembering, and perceiving, and motor skills, such as gross and fine motor movements. Examples of psychomotor performances include driving a car, playing a musical instrument, or performing surgical procedures.

In a medical context, psychomotor performance is often used to assess an individual's ability to perform activities of daily living (ADLs) and instrumental activities of daily living (IADLs), such as bathing, dressing, cooking, cleaning, and managing medications. Deficits in psychomotor performance can be a sign of neurological or psychiatric disorders, such as dementia, Parkinson's disease, or depression.

Assessment of psychomotor performance may involve tests that measure reaction time, coordination, speed, precision, and accuracy of movements, as well as cognitive functions such as attention, memory, and problem-solving skills. These assessments can help healthcare professionals develop appropriate treatment plans and monitor the progression of diseases or the effectiveness of interventions.

"Cerebellar Diseases of Dogs and Cats". Vin.com. Delauche A, Franklin R, Marsella R, Garosi L (February 2019). "Brain: ... Cerebellar hypoplasia - the condition as it occurs in human beings "Cerebellar Hypoplasia Information Page". "Congenital and ... lysosomal storage diseases In 2004, a study was published that linked ketamine to post-anesthetic cerebellar dysfunction in ... cerebellar disease". Vet Stream. ISSN 2398-2950. Hartmann, Katrin (January 2005). "Feline infectious peritonitis". The ...
Parkinson's disease and stroke. More specifically, the neurological diseases that can cause cerebellar degeneration include: ... There are two types of cerebellar degeneration; paraneoplastic cerebellar degeneration, and alcoholic or nutritional cerebellar ... Like any other disease, treatment for cerebellar degeneration is contingent on the underlying cause, unique to each patient. As ... "Cerebellar degeneration". Genetic and Rare Diseases Information Center (GARD) - an NCATS Program. U.S. National Institutes of ...
Millen KJ, Gleeson JG (February 2008). "Cerebellar development and disease". Curr. Opin. Neurobiol. 18 (1): 12-9. doi:10.1016/j ... Cerebellar agenesis can be caused by mutations in the PTF1A gene. Velioglu SK, Kuzeyli K, Ozmenoglu M (September 1998). " ... Cerebellar agenesis is a rare condition in which a brain develops without the cerebellum. The cerebellum controls smooth ... As children with cerebellar agenesis get older, their movements usually improve. It can co-exist with other severe ...
Autosomal Recessive Cerebellar Ataxias. May 1, 2013. Orphonet Journal of Rare Diseases. 17 November 2006 This article ... Orphanet Journal of Rare Diseases "Autosomal Recessive Cerebellar Ataxias." Fracis, Palau Beaudin, Marie; Matilla-Dueñas, ... Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs ... Most cases of autosomal recessive cerebellar ataxia are early onset, usually around the age of 20. People with this type of ...
... (CA), also called cerebellar cortical abiotrophy (CCA), is a genetic neurological disease in animals, ... There are other diseases that lead to cerebellar degeneration, but the loss of Purkinje cells is a clear way to diagnose ... 1985). "Cerebellar Disease in Arabian Horses". Proceedings of the 21st annual convention of the American Association of Equine ... Cerebellar abiotrophy in horses was originally thought to be a form of cerebellar hypoplasia (CH) and was described as such in ...
... (also known as Der Kaloustian-Jarudi-Khoury syndrome) is an autosomally recessive disease that was ... Medicine portal Rare disease "Orphanet: Corneal cerebellar syndrome". Orphanet. October 2006. Retrieved 18 May 2016. "OMIM ... that the disease is different from a disease known as spastic ataxia-corneal dystrophy syndrome that had been found a year ... Corneal-cerebellar syndrome differs from the spastic ataxia-corneal dystrophy syndrome by causing intellectual disability. ...
Cerebellar development and disease. Curr Opin Neurobiol. 2008 Feb;18(1):12-9. Epub 2008 May 29. Doyon J. Motor sequence ... Parkinson's disease, which affects the basal ganglia, has been shown to cause an impairment in the ability to consolidate new ... This points to the importance of the basal ganglia, the primary target of Parkinson's disease, in creating the new sensory/ ... Cerebellar involvement in anticipating the consequences of self-produced actions during bimanual movements. J Neurophysiol. ...
"Cerebellar development and disease". Curr Opin Neurobiol. 18 (1): 12-9. doi:10.1016/j.conb.2008.05.010. PMC 2474776. PMID ... B. Coronal images showing varying degrees of cerebellar hemispheric (one of two halves of a part of the brain) hypoplasia. ... Pontocerebellar hypoplasia is classified as follows: Pontine and cerebellar hypoplasia is also observed in certain phenotypes ... Mental retardation and microcephaly with pontine and cerebellar hypoplasia Millen KJ, Gleeson JG (February 2008). " ...
"Autosomal dominant cerebellar ataxia, deafness, and narcolepsy - About the Disease - Genetic and Rare Diseases Information ... "ZFIN Human Disease: autosomal dominant cerebellar ataxia, deafness and narcolepsy". zfin.org. Retrieved 2022-09-09. " ... "Autosomal dominant cerebellar ataxia, deafness, and narcolepsy". 16 June 2022. "Orphanet: Autosomal dominant cerebellar ataxia ... Autosomal dominant cerebellar ataxia, deafness, and narcolepsy is a rare progressive genetic disorder that primarily affects ...
Lechtenberg, R.; Gilman, S. (1978). "Speech Disorders in Cerebellar Disease" (PDF). Ann. Neurol. 3 (4): 285-290. doi:10.1002/ ... Lyme disease Stroke Tay-Sachs disease, and late-onset Tay-Sachs disease (LOTS) Transient ischemic attack, a 'mini stroke' ... Kent, RD; Netsell, R; Abbs, JH (September 1979). "Acoustic characteristics of dysarthria associated with cerebellar disease". J ... Huntington's disease, Niemann-Pick disease, and Friedreich's ataxia.[citation needed] Toxic and metabolic conditions include: ...
Claus, D; Schöcklmann, HO; Dietrich, HJ (1986). "Long latency muscle responses in cerebellar diseases". European Archives of ... Claus, Detlef; Schocklmann, Dietrich (1986). "Long Latency Muscle Responses in Cerebellar Diseases". European Archives of ... Nerve conduction studies can only diagnose diseases on the muscular and nerve level. They cannot detect disease in the spinal ... Aminoff, [edited by] William F. Brown, Charles F. Bolton, Michael J. (2002). Neuromuscular function and disease : basic, ...
"ZFIN Human Disease: infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly". zfin.org. Retrieved ... "Infantile Cerebral and Cerebellar Atrophy". Jewish Genetic Disease Consortium. Retrieved 2022-07-14. Kaufmann, Rami; ... "Postnatal progressive microcephaly, seizures, and brain atrophy - About the Disease - Genetic and Rare Diseases Information ... Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly is a rare hereditary autosomal recessive ...
"Cerebellar Ataxia in Patients with Mitochondrial DNA Disease". Journal of Neuropathology & Experimental Neurology. 71 (2): 148- ... diabetes Huntington's disease cancer Alzheimer's disease, Parkinson's disease bipolar disorder, schizophrenia, aging and ... Mitochondrial diseases take on unique characteristics both because of the way the diseases are often inherited and because ... Mitochondrial disease can manifest in many different ways. Examples of mitochondrial diseases include: Mitochondrial myopathy ...
Cerebellar dentate nucleus in Alzheimer's disease with myoclonus. [Article]. Dementia and Geriatric Cognitive Disorders, 10(2 ... Canavan's disease: Canavan's disease is a white matter disease due to aspartoacylase deficiency. The dentate nucleus is not ... the deep cerebellar nuclei form a functional unit that provides feedback control of the cerebellar cortex by cerebellar output ... The deep cerebellar nuclei receive the final output from the cerebellar cortex via Purkinje cells in the form of inhibition. ...
In cerebellar diseases, the movements are irregular and inaccurate; in case of the pyramidal tract lesion the motion may be ... With cerebellar disease, the forearm may sway in several cycles. The patient may even strike themself if not guarded.[citation ... is characteristic of cerebellar diseases. Many clinical tests may be employed to test for such disturbances. Alternating ...
"Porencephaly cerebellar hypoplasia internal malformations - About the Disease - Genetic and Rare Diseases Information Center". ... Porencephaly-cerebellar hypoplasia-internal malformations syndrome is a rare autosomal recessive syndrome that mainly affects ... "Orphanet: Porencephaly cerebellar hypoplasia internal malformations syndrome". www.orpha.net. Archived from the original on ... "Porencephaly-cerebellar hypoplasia-internal malformations syndrome (Concept Id: C1832472) - MedGen - NCBI". www.ncbi.nlm.nih. ...
"Delayed Cerebellar Disease and Death after Accidental Exposure to Dimethylmercury". New England Journal of Medicine. 338 (23): ... Fecal matter in particular as it is known to carry many diseases. Many caregivers use gloves while touching the child's ...
"Delayed Cerebellar Disease and Death after Accidental Exposure to Dimethylmercury". New England Journal of Medicine. 338 (23): ... Methylmercury poisoning is also known as Minamata disease. As early as 1865, two workers in the laboratory of Edward Frankland ... Diethylmercury Mercury poisoning Minamata disease Methylmercury "dimethylmercury - Compound Summary". PubChem Compound. US: ... A rare case of Minamata disease". Forensic Science, Medicine and Pathology. 16 (3): 504-509. doi:10.1007/s12024-020-00247-y. ...
"Delayed Cerebellar Disease and Death after Accidental Exposure to Dimethylmercury". New England Journal of Medicine. 338 (23): ...
Another rare disease in the breed is neonatal cerebellar cortical degeneration. Affected puppies are slow, have lower co- ... "Neonatal Cerebellar Cortical Degeneration". Animal Health Trust. Archived from the original on 23 March 2013. Retrieved 13 May ... Beagles are considered a chondrodystrophic breed, meaning that they are prone to types of disk diseases. In rare cases, beagles ... "Frequency of the neonatal cerebellar cortical degeneration (NCCD) mutations in beagles in the UK" (PDF). Kennel Club Genetics ...
"Infantile cerebellar retinal degeneration - About the Disease - Genetic and Rare Diseases Information Center". rarediseases. ... "Orphanet: Infantile cerebellar retinal degeneration". "Infantile Cerebellar-Retinal Degeneration , Hereditary Ocular Diseases ... "Rare Disease Series #17: Infantile Cerebellar-retinal Degeneration". 3billion Blog. 2021-01-15. Retrieved 2022-05-04. Ha, Dong ... Infantile cerebellar retinal degeneration is a rare hereditary neurological disorder which primarily affects the eyes and the ...
"Marie's ataxia": an hereditary disease of the nervous system, with cerebellar ataxia. "Marie-Foix-Alajouanine syndrome": ... Named along with German neurologist Adolph Strümpell (1853-1925). The disease is sometimes referred to as "Bekhterev Disease"; ... Charcot-Marie-Tooth disease Archived 2011-05-14 at the Wayback Machine @ Who Named It Tumblety, Joan (2012). Remaking the Male ... His analysis of the disease was an important contribution in the emerging field of endocrinology. Marie is also credited as the ...
2007). "Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia". J. Hum. Genet. 52 (8): 643-9. doi ... 2006). "16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study". J. Neurol. Sci. 247 (2): 180-6. doi: ... 2005). "Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families". Neurogenetics. 5 (4): ... "An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the ...
Holmes G (1908). "An Attempt to Classify Cerebellar Disease, with a Note on Marie's Hereditary Cerebellar Ataxia". Brain. 30 (4 ... "Psychopathology in patients with degenerative cerebellar diseases: a comparison to Huntington's disease". The American Journal ... An estimated 77% of cases of progressive cerebellar disease are reported to have one or more mental health disorders, and 19% ... Because many SCAs, including SCA1, are polyglutamine diseases and operate by similar mechanisms to Huntington's disease many ...
His wartime observations on gunshot wounds re-awakened his interest in cerebellar disease which led to his classical analysis ... Holmes' observations on gunshot wounds re-awakened his interest in cerebellar disease; this culminated in his classical ... In 1906 he was appointed Physician to the National Hospital for Nervous Diseases, Queen Square, London. At the outbreak of the ... Holmes therefore returned to London and became a resident medical officer at the National Hospital for Nervous Diseases in ...
Chapter 10, "Cerebellar Disease." Elsevier. Nedzelski JM (October 1983). "Cerebellopontine angle tumors: bilateral flocculus ... a tumor of the meninges or membranes that surround the nerves passing through the CPA Cerebellar astrocytoma, a malignant tumor ... Hypertrophic pachymeningitis secondary to IgG4-related disease: case report and review of the literature]". Revista de ...
"The MAZ protein is an autoantigen of Hodgkin's disease and paraneoplastic cerebellar dysfunction". Ann. Neurol. 53 (1): 123-127 ...
CT may show ventricular enlargement due to cerebellar atrophy and white matter disease. Brain biopsy may be necessary to ... Rare diseases, Slow virus diseases, Rare infectious diseases). ... Progression of the disease can be divided into two stages:[ ... the disease can be managed with anticonvulsants, physiotherapy, etc.[citation needed] PRP is very rare and similar to SSPE but ... sometimes myoclonic cerebellar ataxia spastic weakness retinopathy, optic atrophy frank dementia leading to coma spasticity and ...
ET cases that progress to Parkinson's disease are less likely to have had cerebellar problems. Recent neuroimaging studies have ... Louis ED (2014). "'Essential tremor' or 'the essential tremors': is this one disease or a family of diseases?". ... cerebrovascular disease, abnormal bleeding, hemorrhage and/or blood clotting disorders, advanced kidney disease or on dialysis ... Tremor and disease activity can intensify in response to fatigue, strong emotions, low blood sugar, cold and heat, caffeine, ...
... s suffer from an inherited disease, cerebellar ataxia, forcing people to euthanize many puppies. This has been ... Mutant cells suffer disruptions in their endoplasmic reticula, leading to disease. It is hoped that a test will be developed to ... "A SEL1L Mutation Links a Canine Progressive Early-Onset Cerebellar Ataxia to the Endoplasmic Reticulum-Associated Protein ...

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